(Q35210367)

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The Mannich reaction of malonates with simple imines catalyzed by bifunctional cinchona alkaloids: enantioselective synthesis of beta-amino acids

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

The Mannich reaction of malonates with simple imines catalyzed by bifunctional cinchona alkaloids: enantioselective synthesis of beta-amino acids (English)

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

enantioselectivity

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based on heuristic

inferred from title

object named as

Yi Wang

2

0 references

author name string

Jun Song

1

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

Li Deng

3

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Europe PubMed Central

PubMed publication ID

7 August 2017

language of work or name

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publication date

1 May 2006

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Europe PubMed Central

PubMed publication ID

7 August 2017

Journal of the American Chemical Society

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Europe PubMed Central

PubMed publication ID

7 August 2017

128

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Europe PubMed Central

PubMed publication ID

7 August 2017

18

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

6048-6049

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

A direct catalytic asymmetric Mannich-type reaction via a dinuclear zinc catalyst: synthesis of either anti- or syn-alpha-hydroxy-beta-amino ketones

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3172002

28 July 2018

Direct asymmetric anti-Mannich-type reactions catalyzed by a designed amino acid

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3172002

28 July 2018

Enantioselective nitroaldol reaction of alpha-ketoesters catalyzed by cinchona alkaloids

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3172002

28 July 2018

Urea- and thiourea-substituted cinchona alkaloid derivatives as highly efficient bifunctional organocatalysts for the asymmetric addition of malonate to nitroalkenes: inversion of configuration at C9 dramatically improves catalyst performance

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3172002

28 July 2018

Asymmetric Mannich reactions of beta-keto esters with acyl imines catalyzed by cinchona alkaloids

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3172002

28 July 2018

Enantio- and diastereoselective catalytic Mannich-type reaction of a glycine schiff base using a chiral two-center phase-transfer catalyst.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3172002

28 July 2018

Highly enantioselective conjugate addition of nitromethane to chalcones using bifunctional cinchona organocatalysts.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3172002

28 July 2018

Enamine-based organocatalysis with proline and diamines: the development of direct catalytic asymmetric Aldol, Mannich, Michael, and Diels-alder reactions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3172002

28 July 2018

Chiral Brønsted acid-catalyzed direct Mannich reactions via electrophilic activation.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3172002

28 July 2018

Air-stable, storable, and highly efficient chiral zirconium catalysts for enantioselective Mannich-type, aza Diels-Alder, aldol, and hetero Diels-Alder reactions.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3172002

28 July 2018

Enantioselective Mannich-type reaction catalyzed by a chiral Brønsted acid

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3172002

28 July 2018

The direct catalytic asymmetric mannich reaction.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3172002

28 July 2018

Enantioselective Michael Reaction of Malonates to Nitroolefins Catalyzed by Bifunctional Organocatalysts

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3172002

28 July 2018

Recent Developments in the Catalytic Asymmetric Synthesis of α‐ and β‐Amino Acids

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3172002

28 July 2018

Privileged chiral catalysts

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3172002

28 July 2018

The proline-catalyzed direct asymmetric three-component Mannich reaction: scope, optimization, and application to the highly enantioselective synthesis of 1,2-amino alcohols

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3172002

28 July 2018

A General Catalyst for the Asymmetric Strecker Reaction This work was supported by the NIH (GM-43214). A postdoctoral fellowship to M.S.S. (NIH), and a predoctoral fellowship to P.V. sponsored by Alfred Bader are gratefully acknowledged

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3172002

28 July 2018

Direct enantio- and diastereoselective Mannich reactions of malonate and beta-keto esters with N-Boc and N-Cbz aldimines catalysed by a bifunctional cinchonine derivative

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3172002

26 September 2018

anti-selective direct asymmetric Mannich reactions catalyzed by axially chiral amino sulfonamide as an organocatalyst

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3172002

26 September 2018

Bifunctional-thiourea-catalyzed diastereo- and enantioselective aza-Henry reaction

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3172002

26 September 2018

Enantioselective organocatalytic Michael addition of malonate esters to nitro olefins using bifunctional cinchonine derivatives

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3172002

26 September 2018

Direct catalytic asymmetric Mannich-type reactions of N-(2-hydroxyacetyl)pyrrole as an ester-equivalent donor.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3172002

26 September 2018

Direct organocatalytic and highly enantio- and diastereoselective Mannich reactions of alpha-substituted alpha-cyanoacetates

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3172002

26 September 2018

Highly enantioselective thiourea-catalyzed nitro-Mannich reactions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3172002

26 September 2018

Highly enantioselective conjugate addition of malonate and beta-ketoester to nitroalkenes: asymmetric C-C bond formation with new bifunctional organic catalysts based on cinchona alkaloids

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3172002

26 September 2018

The Direct catalytic asymmetric cross-Mannich reaction: a highly enantioselective route to 3-amino alcohols and alpha-amino acid derivatives

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3172002

26 September 2018

Ag-catalyzed asymmetric mannich reactions of enol ethers with aryl, alkyl, alkenyl, and alkynyl imines

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3172002

26 September 2018

Catalytic, asymmetric Mannich-type reactions of N-acylimino esters: reactivity, diastereo- and enantioselectivity, and application to synthesis of N-acylated amino acid derivatives

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3172002

26 September 2018

Asymmetric catalytic Mannich reactions catalyzed by urea derivatives: enantioselective synthesis of beta-aryl-beta-amino acids

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3172002

26 September 2018

Structure-based analysis and optimization of a highly enantioselective catalyst for the strecker reaction

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3172002

26 September 2018

Highly effective chiral ortho-substituted BINAPO ligands (o-BINAPO): applications in Ru-catalyzed asymmetric hydrogenations of beta-aryl-substituted beta-(acylamino)acrylates and beta-keto esters

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3172002

26 September 2018

Enantioselective aza-Henry reaction catalyzed by a bifunctional organocatalyst

1 reference

https://pubmed.ncbi.nlm.nih.gov/16669669

12 December 2020

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Highly enantioselective amination of alpha-substituted alpha-cyanoacetates with chiral catalysts accessible from both quinine and quinidine

1 reference

https://pubmed.ncbi.nlm.nih.gov/16669669

12 December 2020

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Enantioselective catalytic addition of HCN to ketoimines. Catalytic synthesis of quaternary amino acids

1 reference

https://pubmed.ncbi.nlm.nih.gov/16669669

12 December 2020

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Construction of quaternary stereocenters by efficient and practical conjugate additions to alpha,beta-unsaturated ketones with a chiral organic catalyst

1 reference

https://pubmed.ncbi.nlm.nih.gov/16669669

12 December 2020

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Catalytic enantioselective C-C bond forming conjugate additions with vinyl sulfones

1 reference

https://pubmed.ncbi.nlm.nih.gov/16669669

12 December 2020

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The catalytic asymmetric Mannich-type reactions in aqueous media

1 reference

https://pubmed.ncbi.nlm.nih.gov/16669669

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Highly efficient synthesis of beta-amino acid derivatives via asymmetric hydrogenation of unprotected enamines

1 reference

https://pubmed.ncbi.nlm.nih.gov/16669669

12 December 2020

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Stereocontrolled creation of adjacent quaternary and tertiary stereocenters by a catalytic conjugate addition

1 reference

https://pubmed.ncbi.nlm.nih.gov/16669669

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Catalytic Enantioselective Addition to Imines

1 reference

https://pubmed.ncbi.nlm.nih.gov/16669669

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Direct organocatalytic enantioselective mannich reactions of ketimines: an approach to optically active quaternary alpha-amino acid derivatives

1 reference

https://pubmed.ncbi.nlm.nih.gov/16669669

12 December 2020

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Enantioselective conjugate addition of organomagnesium amides to enamidomalonates: synthesis of either enantiomer of beta-amino acid derivatives

1 reference

https://pubmed.ncbi.nlm.nih.gov/16669669

12 December 2020

based on heuristic

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Direct catalytic asymmetric mannich reactions of malonates and beta-keto esters

1 reference

https://pubmed.ncbi.nlm.nih.gov/16669669

12 December 2020

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Recent Progress in the Enantioselective Synthesis of beta-Lactams: Development of the First Catalytic Approaches

1 reference

https://pubmed.ncbi.nlm.nih.gov/16669669

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Catalytic asymmetric addition of beta-ketoesters to various imines by using chiral palladium complexes

1 reference

https://pubmed.ncbi.nlm.nih.gov/16669669

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1021/JA060716F

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

ResearchGate publication ID

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